These are word's examples related to thalassemia. Click on any word to go to its word's detail page. Or, go to the definition of thalassemia.
Hemoglobinopathies such as the sickle cell disorders and thalassemias tend to affect mainly people from certain ethnic minority groups.
As we have seen, screening and prenatal diagnosis are used for thalassemia.
The question remains, however, of how to mediate between autonomy and other goals, such as public health, and welfare of those currently alive who suffer from thalassemia.
One such disease— thalassemia— can now be identified in the foetus as a result of early work on embryonic tissue.
I refer to those who suffer from inherited blood disorders such as sickle sell anaemia or thalassemia major and related haemoglobin disorders.
People with thalassemia make less hemoglobin and have fewer circulating red blood cells than normal, which results in mild or severe anemia.
All thalassemia patients are susceptible to health complications that involve the spleen (which is often enlarged and frequently removed) and gallstones.
In contrast, membrane excess is only relative in patients with iron-deficiency anemia and thalassemia because of the reduced quantity of intracellular hemoglobin.
He handles many important activities, one of them is getting people to donate blood for children with thalassemia.
The two conditions may overlap, however, since some conditions which cause abnormalities in globin proteins (hemoglobinopathy) also affect their production (thalassemia).
Bone marrow transplantation is the only cure and is indicated for patients with severe thalassemia major.
This study showed that long-term treatment did result in a sustainable reduction in the iron burden faced by patients receiving blood transfusions for thalassemia.
Thalassemia results in nontransferrin-bound iron being available in blood as all the transferrin becomes fully saturated.
Scientists focused on diseases caused by single-gene defects, such as cystic fibrosis, haemophilia, muscular dystrophy, thalassemia, and sickle cell anemia.
Alpha thalassemia patients have partial or complete defects in alpha globin production, leading to a relative abundance of beta globin chains in the cell.
